The table below lists the TGFB1 missense variants found in the ExAC population database. Click on each variant for more details, including presence in the 1000 Genomes and Exome Sequencing Project databases, a breakdown by ethnic class and the variant's role in inherited cardiac disease. Use the form below to customise the variant selection. The table can be sorted by variant location, variant type or ExAC frequency.
| No. | Genomic coord.✝ | Variant (CDS)▼ | Variant (Protein) | Variant Type▼ | ExAC frequency▼ | Populations* |
|---|---|---|---|---|---|---|
| 1. | 41858921 | c.29C>T | p.P10L | missense | 0.56228983 | ●●●●●● |
| 2. | 41858876 | c.74G>C | p.R25P | missense | 0.07922884 | ●●●●●● |
| 3. | 41847860 | c.788C>T | p.T263I | missense | 0.02461013 | ●●●●●● |
| 4. | 41858921 | c.29C>G | p.P10R | missense | 0.00064051 | ●●●●●● |
| 5. | 41838037 | c.1010G>C | p.S337T | missense | 0.00063581 | ●●●●●● |
| 6. | 41838160 | c.887G>A | p.R296Q | missense | 0.00038626 | ●●●●●● |
| 7. | 41858864 | c.86G>A | p.G29E | missense | 0.00036210 | ●●●●●● |
| 8. | 41854261 | c.455G>A | p.R152Q | missense | 0.00021418 | ●●●●●● |
| 9. | 41858650 | c.300G>T | p.E100D | missense | 0.00017380 | ●●●●●● |
| 10. | 41850733 | c.553C>T | p.R185W | missense | 0.00015778 | ●●●●●● |
| 11. | 41858612 | c.338T>C | p.M113T | missense | 0.00014836 | ●●●●●● |
| 12. | 41858939 | c.11C>T | p.S4F | missense | 0.00010404 | ●●●●●● |
| 13. | 41858937 | c.13G>C | p.G5R | missense | 0.00010343 | ●●●●●● |
| 14. | 41847926 | c.722C>T | p.T241I | missense | 0.00009128 | ●●●●●● |
| 15. | 41854317 | c.399G>A | p.M133I | missense | 0.00008239 | ●●●●●● |
| 16. | 41854262 | c.454C>T | p.R152W | missense | 0.00008238 | ●●●●●● |
| 17. | 41854294 | c.422G>A | p.R141Q | missense | 0.00007414 | ●●●●●● |
| 18. | 41858892 | c.58G>C | p.V20L | missense | 0.00007329 | ●●●●●● |
| 19. | 41837091 | c.1039A>T | p.N347Y | missense | 0.00007159 | ●●●●●● |
| 20. | 41858865 | c.85G>A | p.G29R | missense | 0.00006279 | ●●●●●● |
| 21. | 41850673 | c.613C>T | p.R205W | missense | 0.00006066 | ●●●●●● |
| 22. | 41858864 | c.86G>C | p.G29A | missense | 0.00006035 | ●●●●●● |
| 23. | 41850657 | c.629G>A | p.R210H | missense | 0.00005942 | ●●●●●● |
| 24. | 41837075 | c.1055C>T | p.A352V | missense | 0.00005758 | ●●●●●● |
| 25. | 41858842 | c.108C>G | p.I36M | missense | 0.00005391 | ●●●●●● |
| 26. | 41850682 | c.604G>A | p.G202R | missense | 0.00005280 | ●●●●●● |
| 27. | 41848104 | c.683G>A | p.R228K | missense | 0.00005042 | ●●●●●● |
| 28. | 41847933 | c.715T>A | p.F239I | missense | 0.00004981 | ●●●●●● |
| 29. | 41858792 | c.158T>C | p.I53T | missense | 0.00004524 | ●●●●●● |
| 30. | 41847857 | c.791C>T | p.P264L | missense | 0.00004142 | ●●●●●● |
| 31. | 41837042 | c.1088C>G | p.P363R | missense | 0.00003841 | ●●●●●● |
| 32. | 41848105 | c.682A>G | p.R228G | missense | 0.00003794 | ●●●●●● |
| 33. | 41838175 | c.872A>C | p.K291T | missense | 0.00003417 | ●●●●●● |
| 34. | 41854274 | c.442G>A | p.V148M | missense | 0.00003295 | ●●●●●● |
| 35. | 41837016 | c.1114C>T | p.R372C | missense | 0.00003120 | ●●●●●● |
| 36. | 41858744 | c.206C>T | p.P69L | missense | 0.00002916 | ●●●●●● |
| 37. | 41850732 | c.554G>A | p.R185Q | missense | 0.00002745 | ●●●●●● |
| 38. | 41838139 | c.908G>A | p.R303H | missense | 0.00002489 | ●●●●●● |
| 39. | 41847884 | c.764G>A | p.R255Q | missense | 0.00002487 | ●●●●●● |
| 40. | 41854264 | c.452C>T | p.S151F | missense | 0.00002471 | ●●●●●● |
| 41. | 41858735 | c.215C>A | p.P72Q | missense | 0.00002433 | ●●●●●● |
| 42. | 41850763 | c.523A>G | p.S175G | missense | 0.00002189 | ●●●●●● |
| 43. | 41858694 | c.256G>T | p.D86Y | missense | 0.00002105 | ●●●●●● |
| 44. | 41858684 | c.266C>T | p.A89V | missense | 0.00001965 | ●●●●●● |
| 45. | 41850747 | c.539G>A | p.R180Q | missense | 0.00001739 | ●●●●●● |
| 46. | 41838181 | c.866C>T | p.T289M | missense | 0.00001729 | ●●●●●● |
| 47. | 41838140 | c.907C>T | p.R303C | missense | 0.00001660 | ●●●●●● |
| 48. | 41847927 | c.721A>G | p.T241A | missense | 0.00001660 | ●●●●●● |
| 49. | 41847867 | c.781A>T | p.M261L | missense | 0.00001657 | ●●●●●● |
| 50. | 41838111 | c.936C>G | p.H312Q | missense | 0.00001653 | ●●●●●● |
| 51. | 41850742 | c.544C>T | p.L182F | missense | 0.00001651 | ●●●●●● |
| 52. | 41838046 | c.1001C>T | p.T334M | missense | 0.00001651 | ●●●●●● |
| 53. | 41850742 | c.544C>G | p.L182V | missense | 0.00001651 | ●●●●●● |
| 54. | 41838077 | c.970G>A | p.G324R | missense | 0.00001650 | ●●●●●● |
| 55. | 41854310 | c.406A>T | p.N136Y | missense | 0.00001648 | ●●●●●● |
| 56. | 41848126 | c.661G>T | p.A221S | missense | 0.00001439 | ●●●●●● |
| 57. | 41850735 | c.551A>G | p.N184S | missense | 0.00001430 | ●●●●●● |
| 58. | 41848101 | c.686A>G | p.D229G | missense | 0.00001245 | ●●●●●● |
| 59. | 41848097 | c.690C>G | p.N230K | missense | 0.00001228 | ●●●●●● |
| 60. | 41858702 | c.248G>C | p.S83T | missense | 0.00001114 | ●●●●●● |
| 61. | 41858690 | c.260G>C | p.R87P | missense | 0.00001030 | ●●●●●● |
| 62. | 41850698 | c.588A>C | p.L196F | missense | 0.00000932 | ●●●●●● |
| 63. | 41858664 | c.286G>A | p.E96K | missense | 0.00000887 | ●●●●●● |
| 64. | 41858658 | c.292G>A | p.E98K | missense | 0.00000879 | ●●●●●● |
| 65. | 41850679 | c.607G>A | p.V203I | missense | 0.00000875 | ●●●●●● |
| 66. | 41858655 | c.295C>A | p.P99T | missense | 0.00000873 | ●●●●●● |
| 67. | 41858613 | c.337A>G | p.M113V | missense | 0.00000872 | ●●●●●● |
| 68. | 41858644 | c.306C>G | p.D102E | missense | 0.00000866 | ●●●●●● |
| 69. | 41850672 | c.614G>A | p.R205Q | missense | 0.00000865 | ●●●●●● |
| 70. | 41850661 | c.625A>C | p.S209R | missense | 0.00000852 | ●●●●●● |
| 71. | 41850658 | c.628C>T | p.R210C | missense | 0.00000849 | ●●●●●● |
| 72. | 41847924 | c.724G>A | p.G242S | missense | 0.00000830 | ●●●●●● |
| 73. | 41847930 | c.718A>C | p.T240P | missense | 0.00000830 | ●●●●●● |
| 74. | 41847930 | c.718A>G | p.T240A | missense | 0.00000830 | ●●●●●● |
| 75. | 41847885 | c.763C>T | p.R255W | missense | 0.00000829 | ●●●●●● |
| 76. | 41847899 | c.749T>G | p.I250S | missense | 0.00000829 | ●●●●●● |
| 77. | 41847900 | c.748A>G | p.I250V | missense | 0.00000829 | ●●●●●● |
| 78. | 41847863 | c.785C>T | p.A262V | missense | 0.00000828 | ●●●●●● |
| 79. | 41838125 | c.922T>C | p.W308R | missense | 0.00000827 | ●●●●●● |
| 80. | 41847797 | c.851A>G | p.Y284C | missense | 0.00000827 | ●●●●●● |
| 81. | 41847830 | c.818G>A | p.S273N | missense | 0.00000827 | ●●●●●● |
| 82. | 41847809 | c.839T>C | p.L280P | missense | 0.00000827 | ●●●●●● |
| 83. | 41847827 | c.821C>T | p.S274F | missense | 0.00000827 | ●●●●●● |
| 84. | 41838037 | c.1010G>A | p.S337N | missense | 0.00000826 | ●●●●●● |
| 85. | 41838094 | c.953A>G | p.H318R | missense | 0.00000826 | ●●●●●● |
| 86. | 41838102 | c.945G>C | p.K315N | missense | 0.00000826 | ●●●●●● |
| 87. | 41838103 | c.944A>G | p.K315R | missense | 0.00000826 | ●●●●●● |
| 88. | 41838050 | c.997G>A | p.D333N | missense | 0.00000825 | ●●●●●● |
| 89. | 41838074 | c.973C>G | p.P325A | missense | 0.00000825 | ●●●●●● |
| 90. | 41838080 | c.967C>T | p.L323F | missense | 0.00000825 | ●●●●●● |
| 91. | 41838055 | c.992G>C | p.S331T | missense | 0.00000825 | ●●●●●● |
| 92. | 41838086 | c.961T>C | p.F321L | missense | 0.00000825 | ●●●●●● |
| 93. | 41838056 | c.991A>G | p.S331G | missense | 0.00000825 | ●●●●●● |
| 94. | 41854273 | c.443T>C | p.V148A | missense | 0.00000824 | ●●●●●● |
| 95. | 41854211 | c.505G>C | p.E169Q | missense | 0.00000824 | ●●●●●● |
| 96. | 41854274 | c.442G>T | p.V148L | missense | 0.00000824 | ●●●●●● |
| 97. | 41854321 | c.395A>G | p.Y132C | missense | 0.00000824 | ●●●●●● |
| 98. | 41854342 | c.374A>G | p.K125R | missense | 0.00000824 | ●●●●●● |
| 99. | 41854261 | c.455G>T | p.R152L | missense | 0.00000824 | ●●●●●● |
| 100. | 41854288 | c.428C>T | p.A143V | missense | 0.00000824 | ●●●●●● |
| 101. | 41854347 | c.369G>T | p.K123N | missense | 0.00000824 | ●●●●●● |
* This highlights the relative frequency of the variant in the ExAC populations - Non-Finnish European, African, East Asian, South Asian, American and Finnish.
Higher frequencies are denoted by darker shades of green, variants absent in a population are coloured light gray.
✝ Genomic coordinates refer to the GRCh37 release of the human genome.